Canonical Allele Identifier: CA1926143169

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863631T= , CM000672.2:g.87863631T= GRCh38
NC_000010.10:g.89623388T= , CM000672.1:g.89623388T= GRCh37
NC_000010.9:g.89613368T= NCBI36
NG_007466.2:g.5194T= , LRG_311:g.5194T=
NG_033079.1:g.4807A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-839T= (PTEN) ENSP00000514759.2:n.-839T=
ENST00000710265.1:c.-839T= (PTEN) ENSP00000518161.1:n.-839T=
ENST00000706954.1:c.-16-823T= (PTEN) ENSP00000516674.1:n.-16-823T=
ENST00000706955.1:c.-839T= (PTEN) ENSP00000516675.1:n.-839T=
ENST00000688158.1:c.-839T= (PTEN) ENSP00000509254.1:n.-839T=
ENST00000688308.1:c.-17+518T= (PTEN) ENSP00000508752.1:n.-17+518T=
ENST00000692337.1:c.73T= (MLDHR) ENSP00000509326.1:p.Ser25=
ENST00000693560.1:c.-319T= (PTEN) ENSP00000509861.1:n.-319T=
ENST00000371953.8:c.-839T= (PTEN) MANE Select ENSP00000361021.3:n.-839T=
ENST00000371953.7:c.-839T= (PTEN) ENSP00000361021.3:n.-839T=
ENST00000610634.1:c.-941T= (PTEN) ENSP00000477517.1:n.-941T=
NM_000314.5:c.-838T= (PTEN) NP_000305.3:n.-838T=
NM_000314.6:c.-838T= (PTEN) NP_000305.3:n.-838T=
NM_001304717.2:c.-319T= (PTEN) NP_001291646.2:n.-319T=
NM_001304718.1:c.-1543T= (PTEN) NP_001291647.1:n.-1543T=
NM_000314.7:c.-838T= (PTEN) NP_000305.3:n.-838T=
NM_001304717.5:c.-319T= (PTEN) NP_001291646.4:n.-319T=
NM_001304718.2:c.-1543T= (PTEN) NP_001291647.1:n.-1543T=
NM_000314.8:c.-839T= (PTEN) MANE Select NP_000305.3:n.-839T=